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The use of homocysteine in the estimation of dehydroascorbic acid.

R. E. Hughes
- 01 Sep 1956 - 
- Vol. 64, Iss: 1, pp 203-208
TLDR
An account is given of a new method, based on the two findings that homocysteine rapidly reduces dehydroascorbic acid at pH 7 0, and that under certain simple conditions 2:6-dichlorophenolindophenol can be used to estimate ascorbic acid in the presence of homocy steine without interference from the latter compound.
Abstract
Two main methods are in current use for the estimation of dehydroascorbic acid. In the one, developed by Roe and his colleagues (Roe & Kuether, 1943; Roe, Mills, Oesterling & Damron, 1948), the dehydroascorbic acid is condensed with 2:4-dinitrophenylhydrazine and the product treated with sulphuric acid to give a red colour, the intensity of which is measured photoelectrically. In a second technique (Tillmans, Hirsch & Siebert, 1932; Eekelen, Emmerie, Josephy & Wolff, 1933; Bessey, 1938), dehydroascorbic acid is measured as acorbic acid after reduction with hydrogen sulphide and removal of excess of reductant. Disadvantages are associated with both methods; they are nonspecific for dehydroascorbic acid, timeand labourconsuming, and in the method involving reduction with hydrogen sulphide it may be difficult to ensure the removal ofexcess ofreductant before estimating the ascorbic acid formed with 2:6-dichlorophenolindophenol. In this paper an account is given ofanew method, based on the two findings that homocysteine rapidly reduces dehydroascorbic acid at pH 7 0, and that under certain simple conditions 2:6-dichlorophenolindophenol can be used to estimate ascorbic acid in the presence of homocysteine without interference from the latter compound.

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TL;DR: The evidence for and the evidence against the presence of the enzyme dehydroascorbate reductase in animal cells is outlined in a balanced way in an attempt to make sense of this continuing controversy.
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Protective systems against active oxygen species in spinach: response to cold acclimation in excess light.

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Changes in the Activities of Anti-Oxidant Enzymes during Exposure of Intact Wheat Leaves to Strong Visible Light at Different Temperatures in the Presence of Protein Synthesis Inhibitors.

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A highly sensitive high-performance liquid chromatography method for the estimation of ascorbic and dehydroascorbic acid in tissues, biological fluids, and foods.

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